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Comparison · NCT00045162-sae

Cisplatin + Irinotecan vs Cisplatin + Etoposide: serious adverse events

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Cisplatin + Irinotecan vs Cisplatin + Etoposide: serious adverse events. Trial comparisons, record NCT00045162-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00045162-sae

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.3330.2840.387wilson
Risk in group 20.09480.06760.131wilson
Risk difference, group 1 minus group 20.2390.1770.298newcombe hybrid score
Risk ratio, group 1 over group 23.522.435.08log
Odds ratio, group 1 over group 24.773.087.39log
Number needed to harm, for one more participant with a serious adverse event on Cisplatin + Irinotecan than on Cisplatin + Etoposide4.193.355.65from the risk difference interval

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Cisplatin + Irinotecan107321EG000
Group 2Cisplatin + Etoposide31327EG001

Harm

What it counts
Total, serious adverse events
Time frame
Patients were evaluated for adverse events prior to the beginning of each cycle of treatment, approximately every 4 weeks, for up to a maximum of 4 cycles (16 weeks).

Source ClinicalTrials.gov

Trial

Title
S0124: Cisplatin Combined With Irinotecan or Etoposide For Extensive-Stage Small Cell Lung Cancer
NCT number
NCT00045162
Phases
PHASE3
Conditions
Lung Cancer
Interventions
cisplatin, etoposide, irinotecan hydrochloride
Lead sponsor
SWOG Cancer Research Network
Results first posted
2013-07-09

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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